This Ability Podcast

In this episode of This Ability Podcast, Mary sits down with Acadiana mother, author, and advocate Emily Wolf to talk about her journey raising her son Seth, who lives with autism and congenital muscular myopathy (RYR1). Emily shares what daily life looks like for their family, the challenges and emotional “dark moments” that many special needs parents face, and the powerful joy that can come from embracing a child’s individuality. Through honesty and reflection, Emily discusses the lessons Seth has taught her about confidence, authenticity, and seeing differences as strengths rather than limitations. Emily also shares the story behind the children’s book she co-created with Seth, A Different Kind of Sea Star, a whimsical underwater tale designed to help children understand that being different is something to celebrate. She reflects on the role faith plays in her parenting, her work with the JoyHeart Collection, and her mission to encourage and uplift other families in the special needs community. This conversation is filled with encouragement, reminding listeners that every child—and every family—has a unique story worth embracing.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, our host Mary Baudoin sits down with Annie Watkins, Site Manager of GiGi’s Playhouse New Orleans, to talk about building a community where individuals with Down syndrome and their families are celebrated, supported, and empowered. From its founding mission to “change the way the world views Down syndrome” to its 62 locations across the U.S. and Mexico, GiGi’s Playhouse delivers free, purposeful programs for participants of all ages — from prenatal support and early childhood classes to teen leadership, adult independence programs, one-on-one tutoring, and speech therapy.Annie shares powerful stories of “best-of-all moments,” explains how GiGi’s removes financial barriers so no family is excluded, and discusses the importance of positive messaging at the time of diagnosis. The conversation also highlights Down Syndrome Awareness Month, World Down Syndrome Day (3/21), volunteer opportunities, the 321 Champion monthly giving program, and hopes for future Louisiana locations. Whether you are a parent, advocate, volunteer, or community supporter, this episode is a reminder that awareness begins with conversation — and acceptance grows through community.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this heartfelt and powerful episode of This Ability Podcast, Sierra Stevens shares her journey as a nurse, a mother of two children with diagnoses, and a woman living with sickle cell disease. Sierra opens up about raising her autistic, non-speaking son Micah and her daughter with ADD, navigating early diagnoses, embracing observation as a parenting tool, and learning to celebrate her children for exactly who they are. She speaks candidly about advocacy in schools, the importance of organizations like Families Helping Families, and how connecting with other parents transformed her sense of isolation into empowerment.Sierra also discusses her own health journey with sickle cell disease, including a recent battle with sickle cell retinopathy and retinal detachment surgeries. With honesty and strength, she reflects on balancing motherhood, marriage, nursing, and board leadership while prioritizing her health and her family’s safety. From elopement prevention and practical safety tools to the healing power of exercise, music, faith, and community, this episode is a reminder that resilience is built one intentional step at a time—and that no parent should walk this path alone.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, Mary sits down with Jo Faulk, a disabled student leader, advocate, and future educator whose lived experience has shaped her understanding of disability, resilience, and voice. Jo reflects on growing up with disability, the influence of her mother’s disability on her own journey, and why advocacy often becomes an “inherent skill” for disabled people. From navigating early self-advocacy to managing the emotional labor that comes with speaking up, Jo offers an honest look at what it means to advocate for yourself while also standing alongside a broader disability community. The conversation also dives into education, leadership, and systemic change. As a history student pursuing teaching certification and the president of her college’s disabled student organization, Jo shares her perspective on where the education system continues to fail disabled students—and how it can be reimagined with disabled voices at the center. She discusses campus advocacy, intersectionality across disability, gender, religion, and society, and what she hopes the disability rights movement prioritizes in the coming decade. This episode is a powerful reminder that disabled students are not just navigating systems—they are actively shaping the future of them.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, host Mary Baudoin sits down with Latasha Holt, a mother, educator, and advocate in Acadiana, to share her family’s journey navigating an ultra-rare medical diagnosis. Latasha opens up about her daughter, Blakelee, who is living with isolated (central) adrenal insufficiency—an exceptionally rare condition affecting approximately one in one million individuals—alongside epilepsy. Together, they break down what this diagnosis means medically, how it differs from more commonly known adrenal disorders, and the challenges of receiving answers when no clear triggering event is present.Latasha also offers an honest look into daily life managing complex medical needs, from medication routines and emergency preparedness to the emotional and psychological realities faced by both parent and child. She reflects on Blakelee’s perspective, the importance of building strong support systems, and the role of advocacy in raising awareness for rare diseases. This conversation highlights resilience, preparedness, and hope—while providing encouragement and practical insight for families navigating similar journeys and for listeners seeking to better understand the lived experience behind rare medical conditions.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, host Mary Baudoin sits down with Elizabeth Duplechain and Amanda Anderson for a heartfelt conversation about Elijah and the journey that surrounds him. Elizabeth, Elijah’s mother, shares what it means to raise a young man diagnosed with Down syndrome, autism, ADD, and ADHD, while navigating advocacy, education, and daily life. Amanda adds her perspective as someone who has walked alongside Elijah and his family, highlighting the importance of support, belief, and community. Although Elijah speaks very little during the interview, his story, presence, and impact are powerfully felt throughout the episode. This conversation serves as an important reminder that ability looks different for everyone—and that unwavering support can make all the difference.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this extended episode of This Ability Podcast, we sit down with Justina Plowden, Miss Wheelchair Louisiana and founder of We Matter, a support and advocacy group for individuals with disabilities across the Acadiana region. Justina shares her journey as a powerful advocate for accessibility, inclusion, and representation. From her experience competing in the Miss Wheelchair America pageant to leading regional conversations around disability rights, Justina speaks candidly about the challenges she’s faced, the community she’s built, and her mission to uplift others through visibility and action.As Miss Wheelchair Louisiana and founder of We Matter, Justina is a true SCI warrior whose work embodies strength, advocacy, and inclusion. In honor of Spinal Cord Injury Awareness, this episode is especially meaningful. She shares her powerful journey as an advocate for accessibility, representation, and community empowerment across Acadiana and beyond. This episode also includes inspiring excerpts from two other guests: Sam Primeaux — who shares how his life was transformed after a motorcycle accident at 17 and how he continues to push forward with grit, faith, and determination. Katie Haynes — who made history as the first person to compete in the Miss United States Agriculture pageant in a wheelchair, and who spreads hope through her nonprofit Together, these stories highlight resilience, leadership, and the power of representation in the disability community.Through We Matter, Justina works to unite individuals across all parishes in Louisiana, focusing on advocacy, peer support, education, and outreach. In this conversation, she reflects on the importance of community empowerment, her commitment to changing perceptions, and how her lived experience fuels her work. Whether you're a caregiver, advocate, or part of the disability community, Justina’s voice is a meaningful reminder that everyone deserves to be seen, heard, and valued.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Extended Episode: Empowerment in Action – Donielle Watkins & Coach Damon VincentIn this extended edition of This Ability Podcast, we revisit our conversation with Donielle Watkins, Executive Director of the DREAMS Foundation of Acadiana, and expand the story by weaving in insights from Coach Damon Vincent, founder of Train Unique.Donielle shares the heartfelt journey behind DREAMS—an organization dedicated to creating inclusive opportunities for individuals with disabilities through sports, art, theater, galas, summer camps, and more. She also highlights their one-of-a-kind meat pie manufacturing food truck, which not only serves delicious food but also employs individuals with disabilities in meaningful ways. Her deep faith and unwavering commitment to community are at the heart of this powerful conversation.But the story doesn’t stop there.Because many DREAMS participants also train with Coach Damon at Train Unique, we’ve enhanced this episode with a special excerpt from his interview. Coach Damon talks about his inclusive approach to fitness, the athletes he trains, and the role that confidence, respect, and tailored support play in helping people reach their full potential—on and off the gym floor.Together, Donielle and Damon offer a shared vision of what’s possible when we invest in ability, inclusion, and community.Tune in for an inspiring, two-voice conversation filled with passion, purpose, and real impact across Acadiana.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this extended episode, we discuss the topic of autism with Season One guest Paul Ganucheau and interview the 2024 Acadiana Teen Spirit Award Winners who are making a difference in the community.🏆 Aubrey David – 9th-grade student at Teurlings Catholic High School🏆 Chloe Songne – 9th-grade student at New Iberia Senior High SchoolAubrey David is an inspiring teenager with a heart for service and a drive to make a meaningful impact in her community. Through her initiative, Aubrey’s Amazing Grace, she has raised thousands of dollars to support families facing hardships, from cancer patients to those in need of housing assistance. Motivated by the example of her former teacher and her own family’s experience with fundraising, Aubrey has turned her compassion into action, organizing bake sales and fundraisers that not only provide financial relief but also bring hope to those in need. Beyond her philanthropic efforts, she is an active member of multiple school organizations and has ambitious goals for the future, aiming to become a chiropractor. Her dedication, empathy, and relentless pursuit of helping others demonstrate wisdom and kindness beyond her years, making her a role model for her peers and a young leader with a bright future ahead.Chloe Songne is an inspirational teenager whose compassion, dedication, and vision for inclusivity set her apart as a true changemaker. As the oldest sibling to six brothers, including two with autism, she is deeply committed to advocating for individuals with special needs. Her work with the Autism Society of Acadiana, her efforts to improve accessibility at festivals, and her involvement in the Very Special Pageant highlight her drive to create a more inclusive world. Beyond her advocacy, Chloe’s leadership as Miss Teen Scott Boudin Festival Queen and her involvement in 4H and Beta Club demonstrate her well-rounded ambition and determination to make a difference. With a heart for service and a passion for education, Chloe’s future is undeniably bright, and she will continue to leave a lasting impact on her community and beyond.We provide some background information about Aubrey's Amazing Grace, the Scott Boudin Festival as well as current statistics in the United States on the topic of autism.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this extended interview, our host Mary Baudoin provides listeners with some background information about the ULL LIFE Program and a little background about our guest Mary Frances Avera.In this inspiring interview, Mary Frances Avera opens up about her rare ZMIZ1 diagnosis, the profound role faith plays in her life, her deep love for animals, and her journey to graduating from the ULL LIFE (Learning Is for Everyone) Program. At end of the episode, our host wraps up the highlights of the conversation and announces the featured guests for next week's episode. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this extended interview, our host Mary Baudoin provides listeners with some background information about the teens featured in this podcast episode. These autistic teens from Red Oaks Coping Cottage School in Lafayette, LA, join us for an engaging and eye-opening conversation. Hear them share what they love about attending Red Oaks School, their experiences with fitting in, their favorite video games, and their unique perspectives on life as autistic individuals. Tune in for an authentic and uplifting discussion that celebrates individuality and community. At the end of the interview, Mary wraps up the conversion with highlights of the interview and provides a sneak peek of guest featured in the next podcast episode, who is Mary Frances Avera.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this extended interview, our host Mary Baudoin recaps Part One of Ashley Benoit Olivier's episode from Season with an introduction before starting the part two content. Ashley gives us an update about her son Drew and the positive impacts of the Early Intervention program. She also talks about Mercy Medical Angels and Miracle Flights (the team that provided airplane trip free of charge for medical appointments), her family's incredible experience while staying at the Ronald McDonald House in Pennsylvania and Drew's involvement with sports, church and school. At the end of the interview, Mary summarizes the organizations that provide free room and board, transportation and other services when traveling with a loved one for medical appointments. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Kim Lanclos Smith shares her experience as the mother and full-time caregiver of her son BJ, a traumatic brain injury (TBI) survivor and artist. They discuss how art has become a tool for healing and expression in their lives.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Join us as we sit down with Rachel Foreman, LCSW, a Lafayette psychotherapist and mom who bravely shares her family’s journey with pediatric bipolar disorder—from the first signs at age five to years of treatment, advocacy, and hard-won stability. Rachel opens up about stigma, school challenges, marriage stress, finding the right clinicians, and why community and honest conversation matter.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Sam Primeaux shares how a life-changing motorcycle accident left him paralyzed at 17 — and how he's faced every day since with grit, faith, and determination. From intensive therapy to strength training and stem cell treatments, Sam opens up about reclaiming independence and redefining possibility.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, Laynie Stevens shares her journey as a college student with cerebral palsy, her leadership as past president of Alpha Delta Pi for students with disabilities & her advocacy work on the Lafayette Mayor-President’s Awareness Committee. As she prepares to graduate with a degree in Accounting, Laynie reflects on accessibility, inclusion & student representation. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this powerful episode of This Ability Podcast, host Mary Baudoin sits down with Jayce Romero, a young DeafBlind advocate from Lafayette, Louisiana, who lives with Usher Syndrome Type 1B. Jayce shares his deeply personal story—from his early diagnosis, educational journey, and family discoveries to his commitment to raising awareness about DeafBlindness. With the help of his interpreter Shirley Delahousie, Jayce offers insight into what life is like navigating the world with both hearing and vision loss, and why visibility and representation matter.Listeners will hear about Jayce’s training experiences at Affiliated Blind of Louisiana and the Helen Keller National Center, his passion for helping others with Usher Syndrome, and his plans to attend Gallaudet University. He also opens up about his battles with depression, his dreams of entering politics or psychology, and how the DeafBlind community has shaped his sense of identity and independence.This episode is a reminder of the resilience and strength within the disability community. Whether you're a parent of a child newly diagnosed with Usher Syndrome, an educator, or simply someone wanting to learn more, Jayce’s story is both educational and inspiring. A full transcription is available on the Buzzsprout website, and a visual podcast version will premiere on YouTube on May 31st.Part Two of Jayce's Episode will launch as the season two finale. Stay tuned to our social media pages for release date. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, we sit down with Justina Plowden, Miss Wheelchair Louisiana and founder of We Matter, a support and advocacy group for individuals with disabilities across the Acadiana region. Justina shares her journey as a powerful advocate for accessibility, inclusion, and representation. From her experience competing in the Miss Wheelchair America pageant to leading regional conversations around disability rights, Justina speaks candidly about the challenges she’s faced, the community she’s built, and her mission to uplift others through visibility and action.Through We Matter, Justina works to unite individuals across all parishes in Louisiana, focusing on advocacy, peer support, education, and outreach. In this conversation, she reflects on the importance of community empowerment, her commitment to changing perceptions, and how her lived experience fuels her work. Whether you're a caregiver, advocate, or part of the disability community, Justina’s voice is a meaningful reminder that everyone deserves to be seen, heard, and valued. Tune in for a story of strength, leadership, and the power of representation.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we sit down with Kristie Curtis — a fierce advocate for disability rights, a passionate community leader, and a devoted mom to three amazing sons, each with unique abilities. Kristie shares her powerful journey into advocacy, her work with LaCAN (Louisiana Council’s Advocacy Network), and the role her unshakable faith has played in helping her overcome life's biggest challenges. Her story is a reminder of the strength found in perseverance, community, and believing in something bigger than yourself.If you’ve ever wondered how to get involved in advocacy, how to navigate the education system, or how to stay grounded through life’s toughest moments, you won’t want to miss this conversation. Tune in now on Apple Podcasts, Spotify, YouTube, or wherever you listen to podcasts — and be inspired by Kristie’s incredible heart, resilience, and commitment to making a difference.  Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, we sit down with Cheryl Laws Tessier, a nurse practitioner, mother, and powerful advocate for the disability community. Cheryl shares her personal journey navigating her son Howard’s autism diagnosis—from early signs and initial dismissals by healthcare providers to securing vital therapies and support services. Her story highlights the importance of trusting your instincts as a parent, understanding your rights, and pushing for early intervention. Cheryl’s persistence led to transformative care for her son, and ultimately, her path into advocacy.As a graduate of the Partners in Policymaking program and former board chair of St. Landry Abilities, Cheryl discusses the critical role of local and state-level advocacy in creating lasting change. She emphasizes the power of personal storytelling to influence policy, the need for support networks like Families Helping Families, and the importance of community connections in rural parishes. With heartfelt honesty, Cheryl also shares how her faith has sustained her through the challenges of parenting and advocacy. This episode is a must-listen for anyone seeking inspiration, empowerment, and practical insights into navigating life as a special needs parent and advocate.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode of This Ability Podcast, we welcome Sylnita Livas-Bougere, an educator, advocate, and devoted mother from Thibodaux, Louisiana. After relocating to Lafayette following Hurricane Ida, Sylnita has dedicated her life to autism awareness and special needs advocacy, inspired by her 13-year-old son, Rain, who was diagnosed with autism at the age of three. She shares her journey of navigating autism, her passion for educating children about neurodiversity, and her work as an author. Her children's books, My Friend Rain and My Friend Rain and The Hurricane, introduce young readers to the world of autism through relatable storytelling, helping them understand and embrace differences with empathy and kindness.  Beyond children's literature, Sylnita has also created resources for parents of children with special needs, including Thriving and Surviving 101: The Journal for Special Needs Parents, a guided journal designed to provide emotional support and an outlet for caregivers. In this episode, she discusses the mental and emotional challenges faced by parents, the importance of community, and her upcoming book My Cup is Half Full: Positive Affirmations for the Special Needs Parent, a collection of daily encouragements and reflections aimed at strengthening and uplifting caregivers. Sylnita’s powerful message of resilience, faith, and advocacy is a must-listen for anyone in the special needs community seeking inspiration and connection.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

🎶 Have you ever wondered how music can heal and bring people together? In this heartfelt episode, I sit down with Vanessa Lomas, founder of TheraCare Music Therapy of Lafayette and president of the Autism Society of Acadiana, to explore the transformative power of music. 🎶 Here’s what we dive into:  🎶 The deep connection between music and life events, like birthdays and celebrations  💊 How music therapy can reduce anxiety and teach calming skills—sometimes even reducing the need for medication  🎸 Adaptive equipment for musical instruments and how Vanessa has taught individuals with unique abilities, including those who are blind  🤝 The support groups offered by the Autism Society of Acadiana for moms, dads, and siblings of individuals with autism  🌟 The vital role volunteers play in supporting the Autism Society’s mission  This episode is packed with inspiring stories and practical insights for anyone interested in the healing power of music or supporting the autism community.  🎧 Tune in now and let’s celebrate the beauty of connection through music! Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, Donielle Watkins shares the inspiring story behind the creation of the DREAMS Foundation of Acadiana and its mission to provide inclusive opportunities for people with disabilities in the Acadiana area. From sports, art, and theater to galas, camps, and more, Donielle highlights the diverse activities that foster connection and empowerment. She also talks about the foundation's innovative meat pie manufacturing food truck, which employs individuals with disabilities, the exciting future of the organization, and how her faith serves as the driving force behind it all. Tune in for a conversation full of hope, vision, and community impact.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we interview the 2024 Acadiana Teen Spirit Award Winners who are making a difference in the community:🏆 Aubrey David – 9th-grade student at Teurlings Catholic High School🏆 Chloe Songne – 9th-grade student at New Iberia Senior High SchoolAubrey David is an inspiring teenager with a heart for service and a drive to make a meaningful impact in her community. Through her initiative, Aubrey’s Amazing Grace, she has raised thousands of dollars to support families facing hardships, from cancer patients to those in need of housing assistance. Motivated by the example of her former teacher and her own family’s experience with fundraising, Aubrey has turned her compassion into action, organizing bake sales and fundraisers that not only provide financial relief but also bring hope to those in need. Beyond her philanthropic efforts, she is an active member of multiple school organizations and has ambitious goals for the future, aiming to become a chiropractor. Her dedication, empathy, and relentless pursuit of helping others demonstrate wisdom and kindness beyond her years, making her a role model for her peers and a young leader with a bright future ahead.Chloe Songne is an inspirational teenager whose compassion, dedication, and vision for inclusivity set her apart as a true changemaker. As the oldest sibling to six brothers, including two with autism, she is deeply committed to advocating for individuals with special needs. Her work with the Autism Society of Acadiana, her efforts to improve accessibility at festivals, and her involvement in the Very Special Pageant highlight her drive to create a more inclusive world. Beyond her advocacy, Chloe’s leadership as Miss Teen Scott Boudin Festival Queen and her involvement in 4H and Beta Club demonstrate her well-rounded ambition and determination to make a difference. With a heart for service and a passion for education, Chloe’s future is undeniably bright, and she will continue to leave a lasting impact on her community and beyond.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this inspiring interview, Mary Frances opens up about her rare ZMIZ1 diagnosis, the profound role faith plays in her life, her deep love for animals, and her journey to graduating from the ULL LIFE (Learning Is for Everyone) Program. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we sit down with autistic teens from Red Oaks Coping in Lafayette, LA, for an engaging and eye-opening conversation. Hear them share what they love about attending Red Oaks School, their experiences with fitting in, their favorite video games, and their unique perspectives on life as autistic individuals. Tune in for an authentic and uplifting discussion that celebrates individuality and community. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this heartwarming episode, we catch up with Ashley as she shares the latest updates about her son Drew and the transformative effects of the Early Intervention program. Ashley opens up about:  The incredible progress Drew has made through Early Intervention and how it’s positively impacted his development.  Her family’s experience with Mercy Medical Angels and Miracle Flights, who provided free airplane trips for Drew’s medical appointments.  Their unforgettable stay at the Ronald McDonald House in Pennsylvania and the support it provided during challenging times.  Drew’s active involvement in sports, church, and school, showing how he’s thriving in every aspect of his life.  Ashley’s story is one of resilience, gratitude, and the power of community support. Tune in to hear about their inspiring journey and the people who’ve helped along the way.  Don’t miss it!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this deeply moving episode, we sit down with Maria Revere, a woman of incredible strength and resilience.  Maria opens up about her journey as a mother, sharing:  Her daughter’s diagnosis of Edward’s Syndrome (Trisomy 18) and the profound impact it had on her family.  The unwavering role of faith in guiding her through life’s toughest challenges. Her own courageous battle with breast cancer and the lessons she’s learned along the way.  Maria’s story is one of hope, perseverance, and the power of faith. Tune in to hear how she navigates life’s hardest moments with grace and strength. You won’t want to miss this inspiring conversation. Listen now!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we’re joined by the inspiring Stephanie Krielow, an advocate making a difference in the special education community.Stephanie shares her powerful journey, including:Her advocacy efforts to secure funding for cameras in SPED classrooms across all parishes, ensuring greater transparency and safety.Practical tips on how anyone can step up and advocate for meaningful change in their communities.The founding of Red Oaks Coping, a resource dedicated to providing support and hope to those in need.The vital role faith plays in her life and mission.Stephanie’s passion and determination are contagious—don’t miss this episode filled with insight, purpose, and hope. Tune in now!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we sit down with the trailblazing Katie Haynes from Youngsville, North Carolina.Katie made history as the first person to compete in the Miss United States Agriculture pageant in a wheelchair, and she shares her inspiring experiences from competing in multiple pageants.  We also discuss:  Her journey living with Gastroparesis and a rare form of dysautonomia called AAG (Autoimmune Autonomic Ganglionopathy).  The incredible work she does through her nonprofit, Smiling While Sending Hope, which spreads joy and awareness by providing care packages to children’s hospitals in North Carolina.  Katie’s mission is to bring smiles, inspire change, and advocate for those with chronic illnesses and special needs. Tune in to hear her story of resilience, advocacy, and hope! Listen Now!About Smiling While Sending Hope:Katie Haynes is the founder of Smiling While Sending Hope, a non-profit dedicated to supporting individuals with chronic illnesses and special needs. A graduate of Southern New Hampshire University, Katie is passionate about making a difference in the disability community through advocacy, care packages, awareness initiatives, and inclusive events.Born and raised in Youngsville, North Carolina, Katie has firsthand experience navigating life with chronic illnesses, including AGG, Gastroparesis, MCAS, CRPS, and others. Her journey inspired her to start Smiling While Sending Hope In 2015 as a 4-H project, which officially became a non-profit four years ago. Under her leadership, the organization has grown to provide birthday programs, toy drives, private events, caregiver support, and the SWSH Ability Club for STEM and creative projects. Through these efforts, Katie has impacted countless families, ensuring that children and adults with disabilities and chronic conditions feel supported, valued, and celebrated.Beyond her advocacy work, Katie is a talented photographer with dreams of working for Disney World or NASCAR. She loves capturing special moments and telling stories through her lens, blending her passion for photography with her dedication to inclusivity and representation. In addition to running Smiling While Sending Hope, she enjoys connecting with her community, speaking at events, and inspiring others to embrace kindness and service.Her mission is simple but powerful: to bring joy, hope, and awareness to those facing medical and physical challenges, ensuring that no one feels alone in their journey. Through her unwavering commitment and resilience, Katie continues to make a lasting impact, one smile at a time.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we welcome Jada Babcock for a heartfelt and inspiring conversation. Jada opens up about her journey as a mother, including:  Her son’s diagnosis of Chromosome 13 Deletion and how it has shaped their family’s life.  Writing her powerful book, An Exceptional Life: A Story of Faith, Missing Chromosomes, & Unconditional Love, which shares their story of resilience, faith, and unconditional love.  Co-creating the JOYHeartCollective with Emily Wolf on Etsy, a venture born from creativity and passion to spread joy.  Jada’s story is a testament to finding purpose, joy, and strength through life’s challenges. Don’t miss this uplifting episode that will leave you inspired and filled with hope! Listen now!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we sit down with Craig Oser, Marketing Director for Special Olympics Louisiana, for an inspiring conversation about the organization’s mission and impact.  Craig shares the exciting new vision for Special Olympics Louisiana, highlighting its commitment to fostering diversity, equity, and inclusion across all communities.  We also explore:  The powerful story behind the Law Enforcement Torch Run  How you can get involved as a volunteer and make a difference  Upcoming fundraisers that support the incredible athletes  Heartwarming success stories of athletes who embody the spirit of Special Olympics  Don’t miss this uplifting and informative episode about the transformative work happening at Special Olympics Louisiana! Listen now and be inspired.  Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Get ready for an inspiring episode featuring Coach Damon, Founder and Owner of Train Unique in Lafayette, Louisiana! Coach Damon shares his journey of creating a gym designed for individuals with special needs. His passion, resilience, and dedication have made him a mentor, friend, and motivator for so many athletes.In this episode, you'll hear about:His bold beginnings (and a "disaster" at age 18!) and the life lessons he’s learned through training at Train Unique.Bonus: Check out the video podcast on our YouTube channel that includes incredible photos of the athletes who bring this gym to life!Listen now and be inspired by Coach Damon’s story!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Listen to This Powerful Episode on Autism Advocacy!  In this episode, we talk with Paul Ganucheau, Board Member with the Autism Society of Acadiana and the first board member on the spectrum. Paul shares his unique perspective on:  The importance of peer support groups  How to be a better advocate and self-advocate  Building partnerships with grassroots advocacy groups like Families Helping Families of Acadiana & LACan  Paul’s insights and dedication to autism advocacy are truly inspiring. Whether you’re an advocate, a self-advocate, or simply looking to learn more, this episode is a must-listen!  Tune in now to hear Paul’s story and his vision for a more inclusive community. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we chat with Jade Viator, Director, and Caroline Billeaudeau, Community and Career Coordinator, of the UL LIFE Program. The UL LIFE (Learning Is For Everyone) Program is a transformative, individualized certificate program designed for young adults with intellectual and developmental disabilities.  Jade and Caroline dive into the program’s core pillars:  Academic growth tailored to each student’s needs  Career development to prepare for meaningful employment  Community involvement and fostering connections  Independent living skills to empower students for the future  The UL LIFE Program offers both a Basic 2-year track and an Advanced 4-year track. Students who complete the program earn a Certificate of Accomplishment through the University of Louisiana College of Education and Human Development. This certificate recognizes their achievements in university courses, LIFE courses, employment training, and community integration.  Tune in to learn more about this life-changing program and its incredible impact on students and their families! Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

In this episode, we sit down with Molly Guidry to talk about her experience raising a teenager with Down syndrome and the incredible accomplishments her daughter has achieved along the way. Molly also highlights the amazing programs offered by the Down Syndrome Association of Acadiana and how they’ve made a difference in their lives.It’s a heartfelt and eye-opening conversation you won’t want to miss! Listen now and be inspired by Molly’s journey and the powerful message of inclusion and support.Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Original recording date: April 2019In this episode, Ashley Benoit Olivier shares her heartfelt story, including: Her son’s rare disease diagnosis and the challenges they’ve faced as a family. The power of Facebook support groups in building a community of hope and connection.   Insights into Trisomy and the incredible journey of her son, Drew.  Ashley’s inspiring perspective offers hope, resilience, and the strength of community. Don’t miss this moving conversation!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Original Recording Date: March 2019In this episode, Liam Doyle dives into:Navigating inaccessible spaces and practical ways to drive meaningful change in accessibility.Highlighting wheelchair-friendly places and events in Acadiana that prioritize inclusion.Expert tips for traveling in a wheelchair, including essential steps for advance preparation to ensure a smooth journey.Whether you’re seeking advice, inspiration, or insight into creating a more accessible world, Liam’s perspective will leave you empowered and informed.Tune in now!Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.

Podcast Recorded in April 2019:In this episode, Molly shares the inspiring story of her daughter with Down syndrome and their incredible journey together. It's a conversation filled with love, resilience, and the beauty of embracing differences. This is an episode that will warm your heart and open your mind.Let Molly’s story remind us all of the power of acceptance and the joy of life’s unexpected paths. In the interview, we also discuss the various types of Down Syndrome: Trisomy 21: About 95% of people with Down syndrome have Trisomy 21.2 With this type of Down syndrome, each cell in the body has 3 separate copies of chromosome 21 instead of the usual 2 copies.Translocation Down syndrome: This type accounts for a small percentage of people with Down syndrome (about 3%). This occurs when an extra part or a whole extra chromosome 21 is present, but it is attached or “trans-located” to a different chromosome rather than being a separate chromosome 21.Mosaic Down syndrome: This type affects about 2% of the people with Down syndrome.2 Mosaic means mixture or combination. For children with mosaic Down syndrome, some of their cells have 3 copies of chromosome 21, but other cells have the typical two copies of chromosome 21. Children with mosaic Down syndrome may have the same features as other children with Down syndrome. However, they may have fewer features of the condition due to the presence of some (or many) cells with a typical number of chromosomes.If you enjoy this episode, please rate this episode or provide us with feedback. Support the showThanks for listening to This Ability Podcast. If you are enjoying our podcast, be sure to like us on Facebook at This Ability Podcast page and subscribe to our YouTube channel.